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Xenical
Clinical Pharmacology
Xenical
In the XENDOS trial, in the overall population, orlistat delayed the onset of type 2 diabetes such that at the end of four years of treatment the cumulative incidence rate of diabetes was 8.3% for the placebo group compared to 5.5% for the orlistat group, p=0.01 (see Table 6 ). This finding was driven by a statistically-significant reduction in the incidence of developing type 2 diabetes in those patients who had impaired glucose tolerance at baseline (Table 6 and Figure 2). Orlistat did not reduce the risk for the development of diabetes in patients with normal glucose tolerance at baseline.
The effect of XENICAL to delay the onset of type 2 diabetes in obese patients with IGT is presumably due to weight loss, and not to any independent effects of the drug on glucose or insulin metabolism. The effect of orlistat on weight loss is adjunctive to diet and exercise.
Table 6: Incidence Rate of Diabetes at Year 4 by OGTT Status
at Baseline*
| OGTT at baseline | Normal | Impaired | All | |||
| Treatment | Placebo | Orlistat | Placebo | Orlistat | Placebo | Orlistat |
| Number of patients* | 1148 | 1235 | 324 | 337 | 1472 | 1572 |
| # pts developing diabetes Life table rate† Observed percent |
16 2.1% 1.4% |
21 1.7% 1.7% |
62 27.2% 19.1% |
48 18.7% 14.2% |
78 8.3% 5.3% |
69 5.5% 4.4% |
| Absolute risk reduction | ||||||
| Life table Observed |
0.4% -0.3% |
8.5% 4.9% |
2.8% 0.9% |
|||
| Relative risk reduction†† | 8% | 42% | 34% | |||
| p-value | 0.79 | < 0.01 | 0.01 | |||
| *Based on patients with a baseline and at
least one follow-up OGTT measurement † Rate adjusted for dropouts ††Computed as (1- hazard ratio) |
||||||
Figure 2: Percentage of Patients Without Diabetes Over Time
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Pediatric Clinical Studies
The effects of XENICAL on body mass index (BMI) and weight loss were assessed in a 54-week multicenter, double-blind, placebo-controlled study in 539 obese adolescents (357 receiving XENICAL 120 mg three times a day, 182 receiving placebo), aged 12 to 16 years. All study participants had a baseline BMI that was 2 units greater than the US weighted mean for the 95th percentile based on age and gender. Body mass index was the primary efficacy parameter because it takes into account changes in height and body weight, which occur in growing children.
During the study, all patients were instructed to take a multivitamin containing fat- soluble vitamins at least 2 hours before or after ingestion of XENICAL. Patients were also maintained on a well-balanced, reduced-calorie diet that was intended to provide 30% of calories from fat. In addition, all patients were placed on a behavior modification program and offered exercise counseling.
Approximately 65% of patients in each treatment group completed the study.
Following one year of treatment, BMI decreased by an average of 0.55 kg/m2 in the XENICAL-treated patients and increased by an average of 0.31 kg/m2 in the placebo- treated patients (p=0.001).
The percentages of patients achieving ≥ 5% and ≥ 10% reduction in BMI and body weight after 52 weeks of treatment for the intent-to-treat population are presented in Table 7.
Table 7 : Percentages of Patients with ≥ 5% and ≥ 10%
Decrease in Body Mass Index and Body Weight After 1-Year Treatment* (Protocol
NM16189)
| Intent-to-Treat Population† | ||||||||
| ≥ 5% Decrease | ≥ 10% Decrease | |||||||
| XENICAL | n | Placebo | n | XENICAL | n | Placebo | n | |
| BMI | 26.5% | 347 | 15.7% | 178 | 13.3% | 347 | 4.5% | 178 |
| Body Weight | 19.0% | 348 | 11.7% | 180 | 9.5% | 348 | 3.3% | 180 |
| * Treatment designates XENICAL 120 mg three times a day plus
diet or placebo plus diet †Last observation carried forward |
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Generic Name: Orlistat 120 mg
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